Blossom S6006Recalls & reported problems
Intra-Lock International, Inc. · Gold & Blue, Ø6.0mm x 6.5mm Blossom™ Implant, Short Collar · Class 2 · Implant
All models of Blossom (66)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 20
- Deaths reported
- 0
- Injuries reported
- 20
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 20 adverse event reports that list this exact device (DI D742S60060), received between Apr 4, 2024 and Mar 26, 2025 — classified as 20 injuries.
The most frequently reported specific device problem is “Failure to Osseointegrate” (20 reports).
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Reports received per month
Most reported problems
Device problems
- Failure to Osseointegrate20
Patient problems
- Insufficient Information20
Recent adverse event reports
The 20 most recent of 20 reports, in the reporter's own words as published by the FDA.
InjuryMar 26, 2025Failure to Osseointegrate; Failure to Osseointegrate
InjuryNov 27, 2024Failure to Osseointegrate; Failure to Osseointegrate
InjuryNov 27, 2024Failure to Osseointegrate; Failure to Osseointegrate
InjuryNov 27, 2024Failure to Osseointegrate; Failure to Osseointegrate
InjuryNov 27, 2024Failure to Osseointegrate; Failure to Osseointegrate
InjuryNov 27, 2024Failure to Osseointegrate; Failure to Osseointegrate
InjuryOct 31, 2024Failure to Osseointegrate; Failure to Osseointegrate
InjuryOct 31, 2024Failure to Osseointegrate; Failure to Osseointegrate
InjuryOct 31, 2024Failure to Osseointegrate; Failure to Osseointegrate
InjuryOct 31, 2024Failure to Osseointegrate; Failure to Osseointegrate
InjuryOct 30, 2024Failure to Osseointegrate; Failure to Osseointegrate
InjuryOct 30, 2024Failure to Osseointegrate; Failure to Osseointegrate
InjuryOct 30, 2024Failure to Osseointegrate; Failure to Osseointegrate
InjurySep 10, 2024Failure to Osseointegrate; Failure to Osseointegrate
InjurySep 10, 2024Failure to Osseointegrate; Failure to Osseointegrate
InjurySep 10, 2024Failure to Osseointegrate; Failure to Osseointegrate
InjurySep 10, 2024Failure to Osseointegrate; Failure to Osseointegrate
InjurySep 10, 2024Failure to Osseointegrate; Failure to Osseointegrate
InjuryAug 14, 2024Failure to Osseointegrate; Failure to Osseointegrate
InjuryApr 4, 2024Failure to Osseointegrate; Failure to Osseointegrate
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- STRAUMANN BONE LEVEL TAPERED IMPLANT SLActive Roxolid BLInstitut Straumann AG · IMPLANT, ENDOSSEOUS, ROOT-FORM22,320 reports
- STRAUMANN BONE LEVEL TAPERED IMPLANT SLActive Roxolid BLInstitut Straumann AG · IMPLANT, ENDOSSEOUS, ROOT-FORM22,267 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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